Systems Engineer

Systems Engineer: Lead will be a part of the Engineering group that is responsible for implementing technical strategies, evaluating, and developing products, and providing a superior level of technical support that benefits the organization. The Systems Engineer: Lead collaborates closely with Engineers, Architects, and Test in the Ventilation business within Sleep and Respiratory Care to develop and commercialize Class 2 medical devices.u00A0u00A0

You will be involved in all system engineering aspects of the Philips V-model, starting with conceptualization, writing requirements, functional and technical design, check & optimize, verification, integration and finally the validation. In your role, you will support system architects and engineers to integrally manage all system engineering aspects in a model-based way supported by the appropriate tools. You will maintain and develop knowledge and expertise resulting in state-of-the-art approaches to serving our customers.u00A0u00A0

You will be involved and expected to lead Sustenance, FDA Remediation systems engineering projects. Hence, experience in Sustenance, FDA remediation systems engineering would be preferred.

In addition, only on specific project need basis, you will lead the systems engineering aspects of Model Based Systems Engineering (MBSE).u00A0 Please note that Sustenance & Remediation projects typically do not require MBSE. As System Engineering Expert and on specific project need basis u2013 you are responsible for the process, method, and tools in the context of model-based system engineering (MBSE) within projects of the Philips businesses globally utilizing the MBSE Modelling tools like Cameo. These projects can cover every phase of the product life cycle, from development, manufacturing, market deployment, operation, and maintenance to phase out. You will also help to deploy capabilities throughout the global company by providing training and coaching to system engineers and system architects.u00A0

Your role:

Incorporates essential operating mechanisms of systems engineering of medical device design and engineering principles and adheres to medical device regulations.u00A0

Defines User Requirements, system requirements, FMEA, architecture, and interfaces to meet product requirements, risk analysis and industry standards conducts system design analysis to select key components and defines control methods and coordinates build and design integrationu00A0

Works together to support product verification and validation planning, resolution of technical integration issues, safety agency interface, system testing and coordination and interfaces with Philips design center.u00A0

Conducts design reviews as part of the product development process to ensure customer requirements are met and the designs are manufacture-able, serviceable, and reliable. In addition, it does the same for subsystem requirements and product integration.u00A0u00A0

As System Engineering Expert, you will:u00A0u00A0

Lead and Support the development of System engineering content in R&D (Research and Development) projects across the business.u00A0u00A0

Manage the system engineering information and its traceability (requirements, risks, design decisions, protocols, results) in the model-based system environment of the businessu00A0

Create adequate requirements and designs for solutions, products, services, and testersu00A0u00A0

Deploy best system engineering practices globally in Philips to R&D project teams or organizations via training & coaching to enhance maturityu00A0

Identify improvement opportunities in Philips businesses proposition and develop actionable proposals, plans and tailored training materials or workshops to address theseu00A0

Manage your activities and services according to good project management practicesu00A0

Coordinate small teams of system engineers if applicableu00A0

Behaviors: The successful candidate will demonstrate the following:u00A0

Leadership: The ability to make things happen by encouraging and channeling the contributions of others recognizing and addressing critical issues in a timely manner and acting as an agent for change and continual improvement when required to achieve results.u00A0u00A0

Accountability/Ownership: Work closely with team members and take ownership u2013 be a mentor to junior engineers u202Fu00A0

Influence: The demonstrated ability to gain acceptance and commitment from others to oneu2019s own beliefs and ideas.u00A0

Negotiating: The ability to construct and maintain a strong bargaining position to ensure positive response and agreement: striving for win-win situations.u00A0

Adaptability: Must possess the ability to understand new concepts quickly and apply them accurately throughout an evolving environment and organize work assignments to meet established timetables.u00A0

Data-driven decision-making: ability to move teams through vague and complex situations. Present complex ideas in a simple manner to resolve issues.u00A0

Relentless focus on Quality and Transparency as an organizational value.

You're the right fit if:

MS or PhD in relevant field including Electrical, Mechanical Engineering, or other related science.u202Fu00A0

A minimum of 8+ years of experience successfully developing complex medical device (hardware, software, consumables) products for acute care/hospital markets is necessary.u00A0

Additional technical knowledge and hands on experience in ventilation will be added advantage.u00A0

Defines User Requirements, system requirements, FMEA, architecture, and interfaces to meet product requirements, risk analysis and industry standards conducts system design analysis to select key components and defines control methods and coordinates build and design integrationu00A0

Experience with Sustenance Engineering, Change review Board, Defect Management

Experience with conducting cross-discipline feasibility and trade off studies to evaluate electronic, mechanical, and pneumatic performance from subsystem to system level for issue resolutionsu00A0u00A0

Analytical and architectural thinking, system view, physical insight, flexibility, and a hands-on mentality to deliver sustainable results and creative solutions.u00A0u00A0

Strong understanding of System Design process including Model-based Design approach and Test-Driven design methodologiesu00A0

Review System Verification and Validation plan/protocols, Test Method Validation (TMV)

Conducting Technical Review & Decision Making

Understanding of global medical device regulatory environments and clearance processes.u00A0

Effective communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team.u00A0

Maintains strict confidentiality of sensitive information.u00A0

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.

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If youu2019re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion .

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Full time